ライフサイエンスコーパス: pico-

1 latable meal-inducible circadian oscillator (PICO) and wheel-inducible circadian oscillator (WICO) ar

2 adee/Profilin, which directly interacts with Pico, and, Mal, a cofactor for serum response factor tha

3 ry and analysis in aqueous samples of nano-, pico-, and femtoliter in volume.

4 tics in microscopic solution volumes (nano-, pico-, and femtoliter range) compared to the usual macro

5 table microscopic aqueous droplets of nano-, pico-, and femtoliter volumes were made and kept under h

6 Acid/base titrations of pico- and femtoliter microsamples have been performed pr

7 aracteristics in microscopic domains (nano-, pico- and femtoliter range) with respect to usual soluti

8 nd proteins (streptavidin and antibodies) at pico- and femtomolar analyte concentrations.

9 By using pico- and femtosecond fluorescence spectroscopy we demon

10 , PhCF3, PhNO2, PhNMe2) were investigated by pico- and nanosecond time-resolved infrared spectroscopy

11 omposition of white truffles (Tuber magnatum Pico) determines its culinary and commercial value.

12 roplets can contain chemicals of interest in pico-, femto-, and attomole amounts or less.

13 eport here that the Drosophila MRL ortholog, pico, is required for tissue and organismal growth.

14 ucleic acid (RNA) from three size fractions (pico-, nano- and micro/mesoplankton), as well as from di

15 sient absorption measurements on the femto-, pico-, nano-, and microsecond time scales and are examin

16 ent methods of RNA amplification, IVT and WT-Pico, produce valid microarray profiles of gene expressi

17 aphy with pinhole incomplete circular orbit (PICO) SPECT imaging of an uncompressed pendant breast wa

18 h density functional theory calculations and pico- through microsecond time-resolved IR spectroscopy.

19 for these experiments: force ranges are from pico- to micronewtons, specimens can be visualized durin

20 ising the rigidity of the domain pair on the pico- to millisecond time-scale.

21 old coating enables capturing the analyte in pico- to nano-molar ranges.

22 Here we show that pico- to nano-second timescale atomic fluctuations in hi

23 mtomole quantities of proteins in individual pico- to nanoliter droplets.

24 Compartmentalization of reactions in pico- to nanoliter water-in-oil droplets in microfluidic

25 noflagellate Alexandrium minutum responds to pico- to nanomolar concentrations of copepodamides with

26 e dynamics of single molecules have required pico- to nanomolar concentrations of fluorophore in orde

27 -containing intermediates and proved potent (pico- to nanomolar range) regulators of both leukocytes

28 In contrast, exposure to gp120 (pico- to nanomolar range, alone or in combination with s

29 easurement of S-nitroso compound levels from pico- to nanomole amounts.

30 IMP-1, increasing 15N relaxation evidence of pico- to nanosecond and micro- to millisecond fluctuatio

31 we also find pronounced changes in both the pico- to nanosecond and the micro- to millisecond time s

32 vide biologically relevant information about pico- to nanosecond backbone motion in proteins.

33 Changes in pico- to nanosecond dynamics indicate that the mutationa

34 dynamics despite having only mild effects on pico- to nanosecond fluctuations as corroborated by NMR.

35 The results show that fast pico- to nanosecond time scale active site loop fluctuat

36 a segment that shows high flexibility on the pico- to nanosecond time scale by (15)N relaxation data.

37 flavin ring) localized dynamics occur on the pico- to nanosecond time scale, while subsequent protein

38 nce large-amplitude internal dynamics on the pico- to nanosecond time scale.

39 surements, which characterize motions on the pico- to nanosecond time scale.

40 idues in the wing are highly flexible on the pico- to nanosecond time scale.

41 Our results show that internal motions on pico- to nanosecond time scales in the backbone of DnaJ(

42 m Sn-based perovskite nanocrystals occurs on pico- to nanosecond time scales via two spectrally disti

43 These motions occur not only on the pico- to nanosecond time scales, but also on the microse

44 large site-to-site variations in dynamics on pico- to nanosecond time scales.

45 ry limited conformational flexibility on the pico- to nanosecond time-scale for both p16 and p18.

46 bility as well as limited flexibility on the pico- to nanosecond time-scale, they display pronounced

47 ase in the extent of protein dynamics on the pico- to nanosecond timescale.

48 nd CRBP II are conformationally rigid on the pico- to nanosecond timescale.

49 g the motion of the permeant molecule on the pico- to nanosecond timescale.

50 ta2 of Cdc42Hs, exhibits low mobility on the pico- to nanosecond timescale.

51 g water transport and relaxation dynamics at pico- to nanosecond timescales and at length scales rele

52 ide binding decreases protein motions in the pico- to nanosecond, and perhaps slower, time range.

53 aestivum Vittad.) and white (Tuber magnatum Pico) truffles.

54 The WT-Ovation Pico System (WT-Pico) was used to amplify 2 ng of pan-neural RNA to prod